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. 2006 Aug;173(4):2151–2164. doi: 10.1534/genetics.105.046730

TABLE 2.

Primers used for amplification and sequencing of the alternative GHR exons (1A, 1B, and 1C) and promoters from bovine genomic DNA

PCR product Forward (5′ → 3′) Reverse (5′ → 3′)
GHR
Exon 1A_1 ATATTCTGGGAGGTGGGTCTC ACAACGCATTGCCTCACATA
Exon 1A_2 CTGGCCTTCACTTCAGTTGG CCCTTTAAAGCAAAGTGACCA
Exon 1BC_1 TCCACACCCCGTCTAGAATC AGCGCGTCATGCTATCTTTT
Exon 1BC_2 CCAAGTCCTTGGTCCTGTGT TGAAAAGCTGTCAACGTGCT
Exon 1BC_3 CGCTGGTCTGTCAAATCTCA CAAACCCAACACTGCCTCTT
Exon 1BC_4 GCTGAGGCCTGTGTCTGAAT TTGGTGCGTGTCACTCTCAT
Exon 1BC_5 CCCTTTCCAGCAGAGAGCTA TCCTCTTCCCATGGCTGA
Exon 1BC_6 GAACGCTTCATCCCAGCTC AAAGTAACAGCCCGATCCTG
Exon 1BC_7 GAACCGCGCTCTCTCTCC CAAAACTGGATTCGGAGGAA
Exon 1BC_8 TCATGGAGTTAGGGGTGACA CTCGAGCAGTTCTGTCAAA